Visvanathan Rizliya, Jayathilake Chathuni, Liyanage Ruvini
Division of Nutritional Biochemistry, National Institute of Fundamental Studies, Hantana Road, Kandy, Sri Lanka; Postgraduate Institute of Science, University of Peradeniya, Sri Lanka.
Division of Nutritional Biochemistry, National Institute of Fundamental Studies, Hantana Road, Kandy, Sri Lanka.
Food Chem. 2016 Nov 15;211:853-9. doi: 10.1016/j.foodchem.2016.05.090. Epub 2016 May 20.
For the first time, a reliable, simple, rapid and high-throughput analytical method for the detection and quantification of α-amylase inhibitory activity using the glucose assay kit was developed. The new method facilitates rapid screening of a large number of samples, reduces labor, time and reagents and is also suitable for kinetic studies. This method is based on the reaction of maltose with glucose oxidase (GOD) and the development of a red quinone. The test is done in microtitre plates with a total volume of 260μL and an assay time of 40min including the pre-incubation steps. The new method is tested for linearity, sensitivity, precision, reproducibility and applicability. The new method is also compared with the most commonly used 3,5-dinitrosalicylic acid (DNSA) method for determining α-amylase activity.
首次开发出一种使用葡萄糖检测试剂盒检测和定量α-淀粉酶抑制活性的可靠、简单、快速且高通量的分析方法。该新方法便于快速筛选大量样品,减少劳动力、时间和试剂消耗,还适用于动力学研究。此方法基于麦芽糖与葡萄糖氧化酶(GOD)的反应以及红色醌的生成。测试在总体积为260μL的微量滴定板中进行,包括预孵育步骤在内的测定时间为40分钟。对新方法进行了线性、灵敏度、精密度、重现性和适用性测试。还将新方法与最常用的用于测定α-淀粉酶活性的3,5-二硝基水杨酸(DNSA)方法进行了比较。